BDBM50215927 4-(1H-pyrrol-2-yl)-1H-imidazo[4,5-c]pyridin-2-amine::CHEMBL230194

SMILES Nc1nc2c(nccc2[nH]1)-c1ccc[nH]1

InChI Key InChIKey=BPADIXRUNSRDOT-UHFFFAOYSA-N

Data  4 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50215927   

TargetMatrix metalloproteinase-14(Human)
Macquarie University

Curated by ChEMBL
LigandPNGBDBM50215927(4-(1H-pyrrol-2-yl)-1H-imidazo[4,5-c]pyridin-2-amin...)
Affinity DataIC50: 8.03E+3nMAssay Description:Inhibition of MMP14 using MOCAc-Pro-Leu-Gly-Leu-A2pr(Dnp)-Ala-Arg- NH2 as substrate preincubated for 10 mins measured after 3 hrs by fluorescence ass...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
Target72 kDa type IV collagenase(Human)
Macquarie University

Curated by ChEMBL
LigandPNGBDBM50215927(4-(1H-pyrrol-2-yl)-1H-imidazo[4,5-c]pyridin-2-amin...)
Affinity DataIC50: 5.01E+4nMAssay Description:Inhibition of human recombinant MMP2 using MOCAc-Pro-Leu-Gly-Leu-A2pr(Dnp)-Ala-Arg- NH2 as substrate preincubated for 10 mins measured after 3 hrs by...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetCyclin-dependent kinase 5 activator 1(Human)
Macquarie University

Curated by ChEMBL
LigandPNGBDBM50215927(4-(1H-pyrrol-2-yl)-1H-imidazo[4,5-c]pyridin-2-amin...)
Affinity DataIC50: 7.00E+4nMAssay Description:Inhibition of human recombinant CDK5/p25 using [gamma-32P] ATP after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetMacrophage metalloelastase(Human)
Kyorin Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50215927(4-(1H-pyrrol-2-yl)-1H-imidazo[4,5-c]pyridin-2-amin...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of MMP12More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed